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1.
Int J Pharm Pharm Sci ; 2020 Aug; 12(8): 136-141
Artículo | IMSEAR | ID: sea-206011

RESUMEN

Objective: Due to the uncertainty about optimal antibiotic treatment, and probably substantial variation in practice, the present study was carried out to determine the bacterial profiles of infected diabetic foot ulcers (DFUs) and also to analyze the prescribing pattern of antibiotics used. Methods: A prospective observational study was carried out in the department of General surgery at a tertiary care teaching hospital, Mangalore. Demographic details and treatment data of 78 patients were collected in a specially designed Proforma, and the data were analyzed using Microsoft Excel. Results: According to Meggit-Wagner's classification, patients admitted with DFUs predominantly belonged to WAGNER 1 category (36%), followed by WAGNER 4 (26%) and WAGNER 2 (22%) categories. Out of 66 culture-positive specimens, 21 (31.8%) had monomicrobial flora, and 45 (68.2%) had polymicrobial flora. A total of 148 organisms were obtained from the specimens. The most common isolates were Staphylococcus aureus (22.3%) and Pseudomonas aeruginosa (17.5%). Ceftriaxone was the most commonly prescribed empirical antibiotic (29%), followed by linezolid (20%), piperacillin-tazobactam (20%), amoxicillin-clavulanic acid (13%), cefoperazone-sulbactam (11%). After the culture and sensitivity (C/S) results, antimicrobials were changed in 74.61% of patients in the preference of Linezolid (51%), Amikacin (27%), Levofloxacin (19%), Ciprofloxacin (17%), Piperacillin-tazobactam (13%), Cefixime (15%), Ceftriaxone (11%) among others. Clindamycin and metronidazole were used to cover anaerobic microorganisms. Conclusion: Most of the microorganisms isolated from DFUs were resistant to many types of antibiotics. Gram-positive organisms were largely sensitive to linezolid and vancomycin, while Gram-negative organisms to amikacin and imipenem. Local treatment of wounds is essential.

2.
3.
Indian Pediatr ; 2009 Jan; 46(1): 75
Artículo en Inglés | IMSEAR | ID: sea-11290
4.
Indian Pediatr ; 2007 Sep; 44(9): 708
Artículo en Inglés | IMSEAR | ID: sea-7101
6.
Indian Pediatr ; 2005 Apr; 42(4): 373-5
Artículo en Inglés | IMSEAR | ID: sea-10940

RESUMEN

Yunis-Varon syndrome is a rare, autosomal recessive syndrome characterized by growth retardation, defective growth of the cranial bones along with complete or partial absence of the clavicles (cleidocranial dysplasia), characteristic facial features, and/or abnormalities of the fingers and/or toes.


Asunto(s)
Anomalías Múltiples , Huesos/anomalías , Anomalías Craneofaciales , Resultado Fatal , Femenino , Dedos/anomalías , Deformidades Congénitas del Pie , Deformidades Congénitas de la Mano , Humanos , Recién Nacido , Masculino , Pezones/anomalías , Polihidramnios , Embarazo , Escroto/anomalías , Síndrome , Dedos del Pie/anomalías
7.
Indian Pediatr ; 2004 Jun; 41(6): 610-3
Artículo en Inglés | IMSEAR | ID: sea-12018

RESUMEN

A 12-year-old male child reported with history of fever for last seven years. Hepatosplenomegaly, hepatic and bone marrow granulomas were the main features. Idiopathic Granulomatous Hepatitis (IGH), a rare syndrome amenable to immunosuppressive therapy was diagnosed.


Asunto(s)
Niño , Fiebre de Origen Desconocido/etiología , Granuloma/complicaciones , Hepatitis/complicaciones , Humanos , Masculino
8.
Indian Pediatr ; 2004 May; 41(5): 510
Artículo en Inglés | IMSEAR | ID: sea-14138
9.
Indian J Exp Biol ; 1989 Jan; 27(1): 41-3
Artículo en Inglés | IMSEAR | ID: sea-55658

RESUMEN

Cyclosporine has been reported to suppress the tensile strength of healing incision wound. Prednisolone, an inducer of hepatic microsomal enzymes, abolished the tensile strength suppressant effect of cyclosporine. Cyclosporine is metabolized by the hepatic cytochrome P-450 enzymes. Induction of microsomal enzymes with phenobarbitone was evaluated for its effect upon the wound healing suppressant effect of cyclosporine. Pretreatment of male rats with phenobarbitone (75 mg/kg/day, ip) for 3 days resulted in alleviating the tensile strength suppressant effect of cyclosporine (5 mg/kg/day, po for 10 days). Phenobarbitone, per se, did not affect the tensile strength. That phenobarbitone prevents cyclosporine induced nephrotoxicity without affecting the humoral immunosuppressant action of cyclosporine has recently been reported. The possibility of modulating microsomal enzymes with phenobarbitone offers another approach in preventing cyclosporine-associated toxicities during immunosuppression.


Asunto(s)
Animales , Ciclosporinas/farmacología , Interacciones Farmacológicas , Masculino , Fenobarbital/farmacología , Ratas , Resistencia a la Tracción/efectos de los fármacos , Cicatrización de Heridas/efectos de los fármacos
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